[go: up one dir, main page]
More Web Proxy on the site http://driver.im/

EP3844242B1 - Materialien für organische elektrolumineszente vorrichtungen - Google Patents

Materialien für organische elektrolumineszente vorrichtungen Download PDF

Info

Publication number
EP3844242B1
EP3844242B1 EP19756194.7A EP19756194A EP3844242B1 EP 3844242 B1 EP3844242 B1 EP 3844242B1 EP 19756194 A EP19756194 A EP 19756194A EP 3844242 B1 EP3844242 B1 EP 3844242B1
Authority
EP
European Patent Office
Prior art keywords
atoms
substituted
radicals
group
aromatic
Prior art date
Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
Active
Application number
EP19756194.7A
Other languages
English (en)
French (fr)
Other versions
EP3844242A1 (de
Inventor
Rouven LINGE
Sebastian Meyer
Lara-Isabel RODRIGUEZ
Aaron Lackner
Current Assignee (The listed assignees may be inaccurate. Google has not performed a legal analysis and makes no representation or warranty as to the accuracy of the list.)
Merck Patent GmbH
Original Assignee
Merck Patent GmbH
Priority date (The priority date is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the date listed.)
Filing date
Publication date
Application filed by Merck Patent GmbH filed Critical Merck Patent GmbH
Publication of EP3844242A1 publication Critical patent/EP3844242A1/de
Application granted granted Critical
Publication of EP3844242B1 publication Critical patent/EP3844242B1/de
Active legal-status Critical Current
Anticipated expiration legal-status Critical

Links

Classifications

    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07D—HETEROCYCLIC COMPOUNDS
    • C07D307/00—Heterocyclic compounds containing five-membered rings having one oxygen atom as the only ring hetero atom
    • C07D307/77—Heterocyclic compounds containing five-membered rings having one oxygen atom as the only ring hetero atom ortho- or peri-condensed with carbocyclic rings or ring systems
    • C—CHEMISTRY; METALLURGY
    • C09—DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
    • C09K—MATERIALS FOR MISCELLANEOUS APPLICATIONS, NOT PROVIDED FOR ELSEWHERE
    • C09K11/00—Luminescent, e.g. electroluminescent, chemiluminescent materials
    • C09K11/06—Luminescent, e.g. electroluminescent, chemiluminescent materials containing organic luminescent materials
    • H—ELECTRICITY
    • H10—SEMICONDUCTOR DEVICES; ELECTRIC SOLID-STATE DEVICES NOT OTHERWISE PROVIDED FOR
    • H10K—ORGANIC ELECTRIC SOLID-STATE DEVICES
    • H10K85/00—Organic materials used in the body or electrodes of devices covered by this subclass
    • H10K85/60—Organic compounds having low molecular weight
    • H10K85/631—Amine compounds having at least two aryl rest on at least one amine-nitrogen atom, e.g. triphenylamine
    • H10K85/633—Amine compounds having at least two aryl rest on at least one amine-nitrogen atom, e.g. triphenylamine comprising polycyclic condensed aromatic hydrocarbons as substituents on the nitrogen atom
    • H—ELECTRICITY
    • H10—SEMICONDUCTOR DEVICES; ELECTRIC SOLID-STATE DEVICES NOT OTHERWISE PROVIDED FOR
    • H10K—ORGANIC ELECTRIC SOLID-STATE DEVICES
    • H10K85/00—Organic materials used in the body or electrodes of devices covered by this subclass
    • H10K85/60—Organic compounds having low molecular weight
    • H10K85/631—Amine compounds having at least two aryl rest on at least one amine-nitrogen atom, e.g. triphenylamine
    • H10K85/636—Amine compounds having at least two aryl rest on at least one amine-nitrogen atom, e.g. triphenylamine comprising heteroaromatic hydrocarbons as substituents on the nitrogen atom
    • H—ELECTRICITY
    • H10—SEMICONDUCTOR DEVICES; ELECTRIC SOLID-STATE DEVICES NOT OTHERWISE PROVIDED FOR
    • H10K—ORGANIC ELECTRIC SOLID-STATE DEVICES
    • H10K85/00—Organic materials used in the body or electrodes of devices covered by this subclass
    • H10K85/60—Organic compounds having low molecular weight
    • H10K85/649—Aromatic compounds comprising a hetero atom
    • H10K85/657—Polycyclic condensed heteroaromatic hydrocarbons
    • H10K85/6574—Polycyclic condensed heteroaromatic hydrocarbons comprising only oxygen in the heteroaromatic polycondensed ring system, e.g. cumarine dyes
    • C—CHEMISTRY; METALLURGY
    • C09—DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
    • C09K—MATERIALS FOR MISCELLANEOUS APPLICATIONS, NOT PROVIDED FOR ELSEWHERE
    • C09K2211/00—Chemical nature of organic luminescent or tenebrescent compounds
    • C09K2211/10—Non-macromolecular compounds
    • C09K2211/1003—Carbocyclic compounds
    • C09K2211/1011—Condensed systems
    • C—CHEMISTRY; METALLURGY
    • C09—DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
    • C09K—MATERIALS FOR MISCELLANEOUS APPLICATIONS, NOT PROVIDED FOR ELSEWHERE
    • C09K2211/00—Chemical nature of organic luminescent or tenebrescent compounds
    • C09K2211/10—Non-macromolecular compounds
    • C09K2211/1018—Heterocyclic compounds
    • H—ELECTRICITY
    • H10—SEMICONDUCTOR DEVICES; ELECTRIC SOLID-STATE DEVICES NOT OTHERWISE PROVIDED FOR
    • H10K—ORGANIC ELECTRIC SOLID-STATE DEVICES
    • H10K2101/00—Properties of the organic materials covered by group H10K85/00
    • H10K2101/10—Triplet emission
    • H—ELECTRICITY
    • H10—SEMICONDUCTOR DEVICES; ELECTRIC SOLID-STATE DEVICES NOT OTHERWISE PROVIDED FOR
    • H10K—ORGANIC ELECTRIC SOLID-STATE DEVICES
    • H10K50/00—Organic light-emitting devices
    • H10K50/10—OLEDs or polymer light-emitting diodes [PLED]
    • H10K50/11—OLEDs or polymer light-emitting diodes [PLED] characterised by the electroluminescent [EL] layers
    • H—ELECTRICITY
    • H10—SEMICONDUCTOR DEVICES; ELECTRIC SOLID-STATE DEVICES NOT OTHERWISE PROVIDED FOR
    • H10K—ORGANIC ELECTRIC SOLID-STATE DEVICES
    • H10K85/00—Organic materials used in the body or electrodes of devices covered by this subclass
    • H10K85/60—Organic compounds having low molecular weight
    • H10K85/615—Polycyclic condensed aromatic hydrocarbons, e.g. anthracene
    • H—ELECTRICITY
    • H10—SEMICONDUCTOR DEVICES; ELECTRIC SOLID-STATE DEVICES NOT OTHERWISE PROVIDED FOR
    • H10K—ORGANIC ELECTRIC SOLID-STATE DEVICES
    • H10K85/00—Organic materials used in the body or electrodes of devices covered by this subclass
    • H10K85/60—Organic compounds having low molecular weight
    • H10K85/615—Polycyclic condensed aromatic hydrocarbons, e.g. anthracene
    • H10K85/626—Polycyclic condensed aromatic hydrocarbons, e.g. anthracene containing more than one polycyclic condensed aromatic rings, e.g. bis-anthracene
    • Y—GENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
    • Y02—TECHNOLOGIES OR APPLICATIONS FOR MITIGATION OR ADAPTATION AGAINST CLIMATE CHANGE
    • Y02E—REDUCTION OF GREENHOUSE GAS [GHG] EMISSIONS, RELATED TO ENERGY GENERATION, TRANSMISSION OR DISTRIBUTION
    • Y02E10/00—Energy generation through renewable energy sources
    • Y02E10/50—Photovoltaic [PV] energy
    • Y02E10/549—Organic PV cells

Definitions

  • the present invention relates to a compound of the formula (1), to the use of the compound in an electronic device, and to an electronic device comprising a compound of the formula (1).
  • the present invention furthermore relates to a process for the preparation of a compound of the formula (1) and to a formulation comprising one or more compounds of the formula (1).
  • the development of functional compounds for use in electronic devices is currently the subject of intensive research.
  • the aim is, in particular, the development of compounds with which improved properties of electronic devices in one or more relevant points can be achieved, such as, for example, power efficiency and lifetime of the device as well as colour coordinates of the emitted light.
  • the term electronic device is taken to mean, inter alia, organic integrated circuits (OICs), organic field-effect transistors (OFETs), organic thin-film transistors (OTFTs), organic light-emitting transistors (OLETs), organic solar cells (OSCs), organic optical detectors, organic photoreceptors, organic field-quench devices (OFQDs), organic light-emitting electrochemical cells (OLECs), organic laser diodes (O-lasers) and organic electroluminescent devices (OLEDs).
  • OICs organic integrated circuits
  • OFETs organic field-effect transistors
  • OFTs organic thin-film transistors
  • OLETs organic light-emitting transistors
  • OSCs organic solar cells
  • OFQDs organic field-quench devices
  • OLEDs organic light-emitting electrochemical cells
  • O-lasers organic laser diodes
  • OEDs organic electroluminescent devices
  • OLEDs Of particular interest is the provision of compounds for use in the last-mentioned electronic devices called OLEDs.
  • the general structure and the functional principle of OLEDs are known to the person skilled in the art and are described, for example, in US 4539507 .
  • Compounds similar to compounds of the invention are disclosed in CN107573306 .
  • Blue-fluorescent emitters known from the prior art are a multiplicity of compounds.
  • Arylamines containing one or more condensed aryl are known from the prior art.
  • Arylamines containing dibenzofuran groups (as disclosed in US 2017/0012214 ) or indenodibenzofuran groups (as disclosed in CN 10753308 or CN 107573925 ) are also known from the prior art.
  • an OLED may comprise different layers, which may be applied either by vapour deposition in a vacuum chamber or by processing from a solution.
  • the processes based on vapour deposition lead to good results, but such processes are complex and expensive. Therefore, there is also a need for OLED materials that can be easily and reliably processed from solution.
  • the materials should have good solubility properties in the solution that comprises them.
  • the OLED materials that are processed from a solution should be able to orientate themselves in the deposited film to improve the overall efficiency of the OLED.
  • orientation means here the horizontal molecular orientation of the compounds, as explained in Zhao et al., Horizontal molecular orientation in solution-processed organic light-emitting diodes, Appl. Phys. Lett. 106063301, 2015 .
  • the present invention is thus based on the technical object of providing compounds which are suitable for use in electronic devices, such as OLEDs, more particularly as blue-fluorescent emitters or matrix materials and, which are suitable for vacuum processing or for solution processing.
  • the invention thus relates to compounds of formula (1), where the following applies to the symbols and indices used:
  • Adjacent substituents in the sense of the present invention are substituents which are bonded to atoms which are linked directly to one another or which are bonded to the same atom.
  • An aryl group in the sense of this invention contains 6 to 60 aromatic ring atoms, preferably 6 to 40 aromatic ring atoms, more preferably 6 to 20 aromatic ring atoms; a heteroaryl group in the sense of this invention contains 5 to 60 aromatic ring atoms, preferably 5 to 40 aromatic ring atoms, more preferably 5 to 20 aromatic ring atoms, at least one of which is a heteroatom.
  • the heteroatoms are preferably selected from N, O and S. This represents the basic definition. If other preferences are indicated in the description of the present invention, for example with respect to the number of aromatic ring atoms or the heteroatoms present, these apply.
  • An aryl group or heteroaryl group here is taken to mean either a simple aromatic ring, i.e. benzene, or a simple heteroaromatic ring, for example pyridine, pyrimidine or thiophene, or a condensed (annellated) aromatic or heteroaromatic polycycle, for example naphthalene, phenanthrene, quinoline or carbazole.
  • a condensed (annellated) aromatic or heteroaromatic polycycle in the sense of the present application consists of two or more simple aromatic or heteroaromatic rings condensed with one another.
  • An aryl or heteroaryl group which may in each case be substituted by the above-mentioned radicals and which may be linked to the aromatic or heteroaromatic ring system via any desired positions, is taken to mean, in particular, groups derived from benzene, naphthalene, anthracene, phenanthrene, pyrene, dihydropyrene, chrysene, perylene, fluoranthene, benzanthracene, benzophenanthrene, tetracene, pentacene, benzopyrene, furan, benzofuran, isobenzofuran, dibenzofuran, thiophene, benzothiophene, isobenzothiophene, dibenzothiophene, pyrrole, indole, isoindole, carbazole, pyridine, quinoline, isoquinoline, acridine, phenanthridine, benzo-5,6-quinoline,
  • aryloxy group in accordance with the definition of the present invention is taken to mean an aryl group, as defined above, which is bonded via an oxygen atom.
  • An analogous definition applies to heteroaryloxy groups.
  • An aromatic ring system in the sense of this invention contains 6 to 60 C atoms in the ring system, preferably 6 to 40 C atoms, more preferably 6 to 20 C atoms.
  • a heteroaromatic ring system in the sense of this invention contains 5 to 60 aromatic ring atoms, preferably 5 to 40 aromatic ring atoms, more preferably 5 to 20 aromatic ring atoms, at least one of which is a heteroatom.
  • the heteroatoms are preferably selected from N, O and/or S.
  • An aromatic or heteroaromatic ring system in the sense of this invention is intended to be taken to mean a system which does not necessarily contain only aryl or heteroaryl groups, but instead in which, in addition, a plurality of aryl or heteroaryl groups may be connected by a non-aromatic unit (preferably less than 10% of the atoms other than H), such as, for example, an sp 3 -hybridised C, Si, N or O atom, an sp 2 -hybridised C or N atom or an sp-hybridised C atom.
  • systems such as 9,9'-spirobifluorene, 9,9'-diaryl-fluorene, triarylamine, diaryl ether, stilbene, etc., are also intended to be taken to be aromatic ring systems in the sense of this invention, as are systems in which two or more aryl groups are connected, for example, by a linear or cyclic alkyl, alkenyl or alkynyl group or by a silyl group.
  • systems in which two or more aryl or heteroaryl groups are linked to one another via single bonds are also taken to be aromatic or heteroaromatic ring systems in the sense of this invention, such as, for example, systems such as biphenyl, terphenyl or diphenyltriazine.
  • An aromatic or heteroaromatic ring system having 5 - 60 aromatic ring atoms, which may in each case also be substituted by radicals as defined above and which may be linked to the aromatic or heteroaromatic group via any desired positions, is taken to mean, in particular, groups derived from benzene, naphthalene, anthracene, benzanthracene, phenanthrene, benzophenanthrene, pyrene, chrysene, perylene, fluoranthene, naphthacene, pentacene, benzopyrene, biphenyl, biphenylene, terphenyl, terphenylene, quaterphenyl, fluorene, spirobifluorene, dihydrophenanthrene, dihydropyrene, tetrahydropyrene, cis- or trans-indenofluorene, truxene, isotruxene, spirotruxene,
  • a straight-chain alkyl group having 1 to 40 C atoms or a branched or cyclic alkyl group having 3 to 40 C atoms or an alkenyl or alkynyl group having 2 to 40 C atoms in which, in addition, individual H atoms or CH 2 groups may be substituted by the groups mentioned above under the definition of the radicals, is preferably taken to mean the radicals methyl, ethyl, n-propyl, i-propyl, n-butyl, i-butyl, s-butyl, t-butyl, 2-methylbutyl, n-pentyl, s-pentyl, cyclopentyl, neopentyl, n-hexyl, cyclohexyl, neohexyl, n-heptyl, cycloheptyl, n-octyl, cyclooctyl, cyclooct
  • An alkoxy or thioalkyl group having 1 to 40 C atoms is preferably taken to mean methoxy, trifluoromethoxy, ethoxy, n-propoxy, i-propoxy, n-butoxy, i-butoxy, s-butoxy, t-butoxy, n-pentoxy, s-pentoxy, 2-methylbutoxy, n-hexoxy, cyclohexyloxy, n-heptoxy, cycloheptyloxy, n-octyloxy, cyclooctyl-oxy, 2-ethylhexyloxy, pentafluoroethoxy, 2,2,2-trifluoroethoxy, methylthio, ethylthio, n-propylthio, i-propylthio, n-butylthio, i-butylthio, s-butylthio, t-butylthio, n-pent
  • the above-mentioned formulation is also intended to be taken to mean that, in the case where one of the two radicals represents hydrogen, the second radical is bonded at the position to which the hydrogen atom was bonded, with formation of a ring. This is illustrated by the following scheme:
  • the group E 1 is on each occurrence, identically or differently, selected from -C(R 0 ) 2 -, -Si(R 0 ) 2 -, -O-, - S-, -N(R 0 )-; or E 1 is a group of formula (E-1), where the symbol * in formula (E-1) indicates the corresponding group E 1 in formula (1) and where E 0 has the same meaning as above.
  • the group E 1 stands for - C(R 0 )2-.
  • the group E 1 stands for a group of formula (E-1) where, E 0 stands for a single bond or -C(R 0 ) 2 -.
  • the group E 2 is on each occurrence, identically or differently, selected from -O- or -S-. Very preferably, the group E 2 stands for -O-.
  • Ar N stands for phenyl, biphenyl, fluorene, spirobifluorene, naphthalene, phenanthrene, dibenzofuran, dibenzothiophene, carbazole, pyridine, pyrimidine, pyrazine, pyridazine, triazine, benzopyridine, benzopyridazine, benzopyrimidine or quinazoline, or for a combination of two to six of these groups, each of which may be substituted by one or more radicals R.
  • Ar N stands for phenyl, biphenyl, fluorene, naphthalene, phenanthrene, dibenzofuran, dibenzothiophene, carbazole or, for a combination of two to six of these groups, each of which may be substituted by one or more radicals R.
  • Ar N stands for a group of one of the formulae (ArN-1) to (ArN-22) as depicted in the table below: where in formulae (ArN-1) to (ArN-22):
  • the compounds of formula (1) are selected from compounds of formula (2), where the symbols Ar N , E 1 , E 2 , R 1 to R 5 and the indices m, n, p, q and r have the same meaning as above.
  • the compounds of formula (1) are selected from compounds of formula (3), where the symbols Ar N , E 2 , R 0 , R 1 to R 5 and the indices m, n, p, q and r have the same meaning as above.
  • the compounds of formula (1) are selected from compounds of formula (4), where the symbols Ar N , E 2 , R 0 , R 1 to R 5 and the indices m, n, p, q and r have the same meaning as above.
  • the compounds of formula (1) are selected from compounds of formulae (4-1) to (4-4), where the symbols Ar N , E 2 , R 0 , R 1 to R 5 have the same meaning as above.
  • the compounds of formulae (4-1) to (4-4) are selected from compounds of formulae (4-1a) to (4-4a), where the symbols Ar N , E 2 , R 0 and R 1 have the same meaning as above.
  • the compounds of formulae (4-1) to (4-4) are selected from compounds of formulae (4-1b) to (4-4b), where the symbols Ar N , E 2 , R 1 and R 0 have the same meaning as above.
  • the compounds of formulae (4-1) to (4-4) are selected from compounds of formulae (4-1c) to (4-4c), where the symbols Ar N , E 2 , R 1 and R 0 have the same meaning as above.
  • the group R 1 stands on each occurrence, identically or differently, for H, D, F, CN, a straight-chain alkyl group having 1 to 40, preferably 1 to 20, more preferably 1 to 10 C atoms or branched or cyclic alkyl group having 3 to 40, preferably 3 to 20, more preferably 3 to 10 C atoms, each of which may be substituted by one or more radicals R, an aromatic or heteroaromatic ring system having 5 to 60, preferably 5 to 40, more preferably 5 to 25, even more preferably 5 to 18 aromatic ring atoms, which may in each case be substituted by one or more radicals R, which may be substituted by one or more radicals R.
  • R 1 is H.
  • the compounds of formula (1) comprise at least one group R 1 selected from an aromatic or heteroaromatic ring system having 5 to 60 aromatic ring atoms.
  • the compounds of formula (1) comprise at least one group R 1 selected from an aromatic or heteroaromatic ring system having 5 to 60 aromatic ring atoms
  • the group R 1 stands preferably for a group selected from phenyl, biphenyl, fluorene, spirobifluorene, naphthalene, phenanthrene, dibenzofuran, dibenzothiophene, carbazole, pyridine, pyrimidine, pyrazine, pyridazine, triazine, benzopyridine, benzopyridazine, benzopyrimidine, quinazoline, or for a combination of two to six of these groups, each of which may be substituted by one or more radicals R.
  • R 1 stands very preferably for a group selected from phenyl, biphenyl, fluorene and naphthalene, each of which may be substituted by one or more radicals R, or for a combination of two to six groups selected from phenyl, biphenyl, fluorene or naphthalene, each of which may be substituted by one or more radicals R.
  • the compounds of formula (1) comprise at least one group R 1 , which stands for a group selected from formulae (R1-1) to (R1-22): where in formulae (R1-1) to (R1-22):
  • the compounds of formula (1) comprise at least one group R 1 , which stands for a group selected from formulae (R1-19) to (R1-22) as represented above.
  • the groups R 0 and R 0a stand on each occurrence, identically or differently, for H, a straight-chain alkyl group having 1 to 10 C atoms or branched or cyclic alkyl group having 3 to 10 C atoms, each of which may be substituted by one or more radicals R, where one or more H atoms may be replaced by D, F, Cl, Br, I, CN or NO 2 , an aromatic or heteroaromatic ring system having 5 to 18 aromatic ring atoms, which may in each case be substituted by one or more radicals R, where two adjacent substituents R 0 and/or R 0a may form a mono- or polycyclic, aliphatic ring system or aromatic ring system, which may be substituted by one or more radicals R.
  • the groups R 0 and/or R 0a stand on each occurrence, identically or differently, for a straight-chain alkyl group having 1 to 10 C atoms, which may be substituted by one or more radicals R, or an aromatic or heteroaromatic ring system having 5 to 18 aromatic ring atoms, which may in each case be substituted by one or more radicals R, where two adjacent substituents R 0 may form a mono- or polycyclic, aliphatic ring system or aromatic ring system, which may be substituted by one or more radicals R.
  • R 0 stands on each occurrence, identically or differently, for a methyl or a phenyl group, which may be substituted by one or more radicals R.
  • the group R 0a stand on each occurrence, identically or differently, for a straight-chain alkyl group having 1 to 10 C atoms, which may be substituted by one or more radicals R.
  • the groups of formulae (ArN-12) and (R1-12) comprise 1 or 2 groups R 0a , which stand(s) for a straight-chain alkyl group having 3 to 10, preferably 5 to 10, more preferably 6 to 10 C atoms and the groups or formulae (ArN-19) to (ArN-22), (R1-19) to (R1-22) comprise 1, 2, 3 or 4 groups R 0a , which stand(s) for a straight-chain alkyl group having 3 to 10, preferably 5 to 10, more preferably 6 to 10 C atoms.
  • R 2 to R 5 stand on each occurrence, identically or differently, for H, D, F, CN, a straight-chain alkyl group having 1 to 40, preferably 1 to 20, more preferably 1 to 10 C atoms or a branched or cyclic alkyl group having 3 to 40, preferably 3 to 20, more preferably 3 to 10 C atoms, each of which may be substituted by one or more radicals R, or an aromatic or heteroaromatic ring system having 5 to 18 aromatic ring atoms, which may in each case be substituted by one or more radicals R.
  • R 2 to R 5 stand on each occurrence, identically or differently, for H, a straight-chain alkyl group having 1 to 10 C atoms or a branched or cyclic alkyl group having 3 to 10 C atoms, each of which may be substituted by one or more radicals R, or an aromatic or heteroaromatic ring system having 5 to 18 aromatic ring atoms, which may in each case be substituted by one or more radicals R.
  • R 2 to R 5 stand for H.
  • R stands on each occurrence, identically or differently, for H, D, F, Cl, Br, I, CN, a straight-chain alkyl group having 1 to 10 C atoms or branched or cyclic alkyl group having 3 to 10 C atoms, or an aromatic or heteroaromatic ring system having 5 to 18 C atoms.
  • the compounds according to the invention can be prepared by synthesis steps known to the person skilled in the art, such as, for example, bromination, Suzuki coupling, Ullmann coupling, Hartwig-Buchwald coupling, etc.
  • An example of a suitable synthesis process is depicted in general terms in Schemes 1 and 2 below.
  • the present invention therefore relates to a process for the synthesis of the compounds according to the invention, comprising a step where an aminated oxatruxene derivative reacts with an indenodibenzofuran derivative.
  • formulations of the compounds according to the invention are necessary. These formulations can be, for example, solutions, dispersions or emulsions. It may be preferred to use mixtures of two or more solvents for this purpose.
  • Suitable and preferred solvents are, for example, toluene, anisole, o-, m- or p-xylene, methyl benzoate, mesitylene, tetralin, veratrol, THF, methyl-THF, THP, chlorobenzene, dioxane, phenoxytoluene, in particular 3-phenoxytoluene, (-)-fenchone, 1,2,3,5-tetramethylbenzene, 1,2,4,5-tetramethylbenzene, 1-methylnaphthalene, 2-methylbenzothiazole, 2-phenoxyethanol, 2-pyrrolidinone, 3-methylanisole, 4-methylanisole, 3,4-dimethylanisole, 3,5-dimethylanisole, acetophenone, ⁇ -terpineol, benzothiazole, butyl benzoate, cumene, cyclohexanol, cyclohexanone, cyclohexylbenzene, decalin, do
  • the present invention therefore furthermore relates to a formulation comprising a compound according to the invention and at least one further compound.
  • the further compound may be, for example, a solvent, in particular one of the above-mentioned solvents or a mixture of these solvents.
  • the further compound may also be at least one further organic or inorganic compound which is likewise employed in the electronic device, for example an emitting compound, in particular a phosphorescent dopant, and/or a further matrix material. Suitable emitting compounds and further matrix materials are indicated below in connection with the organic electroluminescent device.
  • This further compound may also be polymeric.
  • An electronic device here is taken to mean a device which comprises at least one layer which comprises at least one organic compound.
  • the component here may also comprise inorganic materials or also layers built up entirely from inorganic materials.
  • the present invention therefore furthermore relates to the use of the compounds or mixtures according to the invention in an electronic device, in particular in an organic electroluminescent device.
  • the present invention again furthermore relates to an electronic device comprising at least one of the compounds or mixtures according to the invention mentioned above.
  • the preferences stated above for the compound also apply to the electronic devices.
  • the electronic device is preferably selected from the group consisting of organic electroluminescent devices (OLEDs, PLEDs), organic integrated circuits (O-ICs), organic field-effect transistors (O-FETs), organic thin-film transistors (O-TFTs), organic light-emitting transistors (O-LETs), organic solar cells (O-SCs), organic dye-sensitised solar cells, organic optical detectors, organic photoreceptors, organic field-quench devices (O-FQDs), light-emitting electrochemical cells (LECs), organic laser diodes (O-lasers) and "organic plasmon emitting devices” ( D. M. Koller et al., Nature Photonics 2008, 1-4 ), preferably organic electroluminescent devices (OLEDs, PLEDs), in particular phosphorescent OLEDs.
  • OLEDs organic electroluminescent devices
  • PLEDs organic integrated circuits
  • O-FETs organic field-effect transistors
  • OF-TFTs organic thin-film
  • the organic electroluminescent device comprises a cathode, an anode and at least one emitting layer. Apart from these layers, it may also comprise further layers, for example in each case one or more hole-injection layers, hole-transport layers, hole-blocking layers, electron-transport layers, electron-injection layers, exciton-blocking layers, electron-blocking layers and/or charge-generation layers. It is likewise possible for interlayers, which have, for example, an exciton-blocking function, to be introduced between two emitting layers. However, it should be pointed out that each of these layers does not necessarily have to be present.
  • the organic electroluminescent device here may comprise one emitting layer or a plurality of emitting layers.
  • a plurality of emission layers are present, these preferably have in total a plurality of emission maxima between 380 nm and 750 nm, resulting overall in white emission, i.e. various emitting compounds which are able to fluoresce or phosphoresce are used in the emitting layers.
  • various emitting compounds which are able to fluoresce or phosphoresce are used in the emitting layers.
  • Particular preference is given to systems having three emitting layers, where the three layers exhibit blue, green and orange or red emission (for the basic structure see, for example, WO 2005/011013 ).
  • These can be fluorescent or phosphorescent emission layers or hybrid systems, in which fluorescent and phosphorescent emission layers are combined with one another.
  • an organic electroluminescent device comprising a compound of the formula (1) or in accordance with the preferred embodiments as fluorescent emitters, emitters showing TADF (Thermally Activated Delayed Fluorescence), matrix material for fluorescent emitters.
  • TADF Thermally Activated Delayed Fluorescence
  • an organic electroluminescent device comprising a compound of the formula (1) or in accordance with the preferred embodiments as fluorescent emitters, more particularly blue-emitting fluorescent compound.
  • the compounds of formula (1) can also be employed in an electron-transport layer and/or in an electron-blocking or exciton-blocking layer and/or in a hole-transport layer, depending on the precise substitution.
  • the preferred embodiments indicated above also apply to the use of the materials in organic electronic devices.
  • the compound according to the invention is particularly suitable for use as blue-emitting emitter compound.
  • the electronic device concerned may comprise a single emitting layer comprising the compound according to the invention or it may comprise two or more emitting layers.
  • the further emitting layers here may comprise one or more compounds according to the invention or alternatively other compounds.
  • the compound according to the invention is employed as a fluorescent emitting compound in an emitting layer, it is preferably employed in combination with one or more matrix materials.
  • a matrix material here is taken to mean a material which is present in the emitting layer, preferably as the principal component, and which does not emit light on operation of the device.
  • the proportion of the emitting compound in the mixture of the emitting layer is between 0.1 and 50.0%, preferably between 0.5 and 20.0%, particularly preferably between 1.0 and 10.0%.
  • the proportion of the matrix material or matrix materials is between 50.0 and 99.9%, preferably between 80.0 and 99.5%, particularly preferably between 90.0 and 99.0%.
  • the specifications of the proportions in % are, for the purposes of the present application, taken to mean % by vol. if the compounds are applied from the gas phase and % by weight if the compounds are applied from solution.
  • Preferred matrix materials for use in combination with fluorescent emitting compounds are selected from the classes of the oligoarylenes (for example 2,2',7,7'-tetraphenylspirobifluorene in accordance with EP 676461 or dinaphthylanthracene), in particular the oligoarylenes containing condensed aromatic groups, the oligoarylenevinylenes (for example DPVBi or spiro-DPVBi in accordance with EP 676461 ), the polypodal metal complexes (for example in accordance with WO 2004/081017 ), the hole-conducting compounds (for example in accordance with WO 2004/058911 ), the electron-conducting compounds, in particular ketones, phosphine oxides, sulfoxides, etc.
  • the oligoarylenes for example 2,2',7,7'-tetraphenylspirobifluorene in accordance with EP 676461 or dinaphthylanth
  • Particularly preferred matrix materials are selected from the classes of the oligoarylenes, comprising naphthalene, anthracene, benzanthracene and/or pyrene or atropisomers of these compounds, the oligoarylenevinylenes, the ketones, the phosphine oxides and the sulfoxides.
  • Very particularly preferred matrix materials are selected from the classes of the oligoarylenes, comprising anthracene, benzanthracene, benzophenanthrene and/or pyrene or atropisomers of these compounds.
  • An oligoarylene in the sense of this invention is intended to be taken to mean a compound in which at least three aryl or arylene groups are bonded to one another.
  • the compound according to the invention is employed as a fluorescent emitting compound in an emitting layer, it may be employed in combination with one or more other fluorescent emitting compounds.
  • Preferred fluorescent emitters are selected from the class of the arylamines.
  • An arylamine in the sense of this invention is taken to mean a compound which contains three substituted or unsubstituted aromatic or heteroaromatic ring systems bonded directly to the nitrogen. At least one of these aromatic or heteroaromatic ring systems is preferably a condensed ring system, particularly preferably having at least 14 aromatic ring atoms.
  • Preferred examples thereof are aromatic anthracenamines, aromatic anthracenediamines, aromatic pyrenamines, aromatic pyrenediamines, aromatic chrysenamines or aromatic chrysenediamines.
  • An aromatic anthracenamine is taken to mean a compound in which one diarylamino group is bonded directly to an anthracene group, preferably in the 9-position.
  • An aromatic anthracenediamine is taken to mean a compound in which two diarylamino groups are bonded directly to an anthracene group, preferably in the 9,10-position.
  • Aromatic pyrenamines, pyrenediamines, chrysenamines and chrysenediamines are defined analogously thereto, where the diarylamino groups are preferably bonded to the pyrene in the 1-position or in the 1,6-position.
  • emitters are indenofluorenamines or indenofluorenediamines, for example in accordance with WO 2006/108497 or WO 2006/122630 , benzoindenofluorenamines or benzoindenofluorenediamines, for example in accordance with WO 2008/006449 , and dibenzoindenofluorenamines or dibenzoindeno-fluorenediamines, for example in accordance with WO 2007/140847 , and the indenofluorene derivatives containing condensed aryl groups which are disclosed in WO 2010/012328 .
  • Still further preferred emitters are benzanthracene derivatives as disclosed in WO 2015/158409 , anthracene derivatives as disclosed in WO 2017/036573 , fluorene dimers like in WO 2016/150544 or phenoxazine derivatives as disclosed in WO 2017/028940 and WO 2017/028941 .
  • Preference is likewise given to the pyrenarylamines disclosed in WO 2012/048780 and WO 2013/185871 .
  • the compounds according to the invention can also be employed in other layers, for example as hole-transport materials in a hole-injection or hole-transport layer or electron-blocking layer or as matrix materials in an emitting layer, preferably as matrix materials for phosphorescent emitters.
  • the compound of the formula (I) is employed as hole-transport material in a hole-transport layer, a hole-injection layer or an electron-blocking layer, the compound can be employed as pure material, i.e. in a proportion of 100%, in the hole-transport layer, or it can be employed in combination with one or more further compounds.
  • the organic layer comprising the compound of the formula (I) then additionally comprises one or more p-dopants.
  • the p-dopants employed in accordance with the present invention are preferably organic electron-acceptor compounds which are able to oxidise one or more of the other compounds of the mixture.
  • p-dopants are the compounds disclosed in WO 2011/073149 , EP 1968131 , EP 2276085 , EP 2213662 , EP 1722602 , EP 2045848 , DE 102007031220 , US 8044390 , US 8057712 , WO 2009/003455 , WO 2010/094378 , WO 2011/120709 , US 2010/0096600 and WO 2012/095143 .
  • the phosphorescent emitter is preferably selected from the classes and embodiments of phosphorescent emitters indicated below. Furthermore, one or more further matrix materials are preferably present in the emitting layer in this case.
  • So-called mixed-matrix systems of this type preferably comprise two or three different matrix materials, particularly preferably two different matrix materials. It is preferred here for one of the two materials to be a material having hole-transporting properties and for the other material to be a material having electron-transporting properties.
  • the compound of the formula (I) is preferably the material having hole-transporting properties.
  • the desired electron-transporting and hole-transporting properties of the mixed-matrix components may also be combined mainly or completely in a single mixed-matrix component, where the further mixed-matrix component or components satisfy other functions.
  • the two different matrix materials may be present here in a ratio of 1:50 to 1:1, preferably 1:20 to 1:1, particularly preferably 1:10 to 1:1 and very particularly preferably 1:4 to 1:1.
  • Mixed-matrix systems are preferably employed in phosphorescent organic electroluminescent devices. Further details on mixed-matrix systems are contained, inter alia, in the application WO 2010/108579 .
  • Particularly suitable matrix materials which can be used as matrix components of a mixed-matrix system in combination with the compounds according to the invention are selected from the preferred matrix materials for phosphorescent emitters indicated below or the preferred matrix materials for fluorescent emitters, depending on what type of emitter compound is employed in the mixed-matrix system.
  • Suitable phosphorescent emitters are, in particular, compounds which emit light, preferably in the visible region, on suitable excitation and in addition contain at least one atom having an atomic number greater than 20, preferably greater than 38 and less than 84, particularly preferably greater than 56 and less than 80.
  • the phosphorescent emitters used are preferably compounds which contain copper, molybdenum, tungsten, rhenium, ruthenium, osmium, rhodium, iridium, palladium, platinum, silver, gold or europium, in particular compounds which contain iridium, platinum or copper.
  • luminescent iridium, platinum or copper complexes are regarded as phosphorescent compounds.
  • Examples of the phosphorescent emitters described above are revealed by the applications WO 2000/70655 , WO 2001/41512 , WO 2002/02714 , WO 2002/15645 , EP 1191613 , EP 1191612 , EP 1191614 , WO 2005/033244 , WO 2005/019373 and US 2005/0258742 .
  • all phosphorescent complexes as used in accordance with the prior art for phosphorescent OLEDs and as are known to the person skilled in the art in the area of organic electroluminescent devices are suitable for use in the devices according to the invention.
  • the person skilled in the art will also be able to employ further phosphorescent complexes without inventive step in combination with the compounds according to the invention in OLEDs.
  • Preferred matrix materials for phosphorescent emitters are aromatic ketones, aromatic phosphine oxides or aromatic sulfoxides or sulfones, for example in accordance with WO 2004/013080 , WO 2004/093207 , WO 2006/005627 or WO 2010/006680 , triarylamines, carbazole derivatives, for example CBP (N,N-biscarbazolylbiphenyl) or the carbazole derivatives disclosed in WO 2005/039246 , US 2005/0069729 , JP 2004/288381 , EP 1205527 or WO 2008/086851 , indolocarbazole derivatives, for example in accordance with WO 2007/063754 or WO 2008/056746 , indenocarbazole derivatives, for example in accordance with WO 2010/136109 , WO 2011/000455 or WO 2013/041176 , azacarbazole derivatives, for example in accordance with EP 1617710
  • suitable charge-transport materials are, for example, the compounds disclosed in Y. Shirota et al., Chem. Rev. 2007, 107(4), 953-1010 , or other materials as are employed in these layers in accordance with the prior art.
  • Materials which can be used for the electron-transport layer are all materials as are used in accordance with the prior art as electron-transport materials in the electron-transport layer. Particularly suitable are aluminium complexes, for example Alq 3 , zirconium complexes, for example Zrq 4 , lithium complexes, for example Liq, benzimidazole derivatives, triazine derivatives, pyrimidine derivatives, pyridine derivatives, pyrazine derivatives, quinoxaline derivatives, quinoline derivatives, oxadiazole derivatives, aromatic ketones, lactams, boranes, diazaphosphole derivatives and phosphine oxide derivatives. Furthermore suitable materials are derivatives of the above-mentioned compounds, as disclosed in JP 2000/053957 , WO 2003/060956 , WO 2004/028217 , WO 2004/080975 and WO 2010/072300 .
  • Preferred hole-transport materials which can be used in a hole-transport, hole-injection or electron-blocking layer in the electroluminescent device according to the invention are indenofluorenamine derivatives (for example in accordance with WO 06/122630 or WO 06/100896 ), the amine derivatives disclosed in EP 1661888 , hexaazatriphenylene derivatives (for example in accordance with WO 01/049806 ), amine derivatives containing condensed aromatic rings (for example in accordance with US 5,061,569 ), the amine derivatives disclosed in WO 95/09147 , monobenzoindenofluorenamines (for example in accordance with WO 08/006449 ), dibenzoindenofluorenamines (for example in accordance with WO 07/140847 ), spirobifluorenamines (for example in accordance with WO 2012/034627 or WO 2013/120577 ), fluorenamines (for example in accordance with the as applications EP 28750
  • the cathode of the organic electroluminescent device preferably comprises metals having a low work function, metal alloys or multilayered structures comprising various metals, such as, for example, alkaline-earth metals, alkali metals, main-group metals or lanthanoids (for example Ca, Ba, Mg, Al, In, Mg, Yb, Sm, etc.). Also suitable are alloys comprising an alkali metal or alkaline-earth metal and silver, for example an alloy comprising magnesium and silver.
  • further metals which have a relatively high work function such as, for example, Ag or Al
  • lithium quinolinate (LiQ) can be used for this purpose.
  • the layer thickness of this layer is preferably between 0.5 and 5 nm.
  • the anode preferably comprises materials having a high work function.
  • the anode preferably has a work function of greater than 4.5 eV vs. vacuum. Suitable for this purpose are on the one hand metals having a high redox potential, such as, for example, Ag, Pt or Au.
  • metal/metal oxide electrodes for example Al/Ni/NiO x , Al/PtO x ) may also be preferred.
  • at least one of the electrodes must be transparent or partially transparent in order to facilitate either irradiation of the organic material (organic solar cells) or the coupling-out of light (OLEDs, O-lasers).
  • Preferred anode materials here are conductive mixed metal oxides. Particular preference is given to indium tin oxide (ITO) or indium zinc oxide (IZO). Preference is furthermore given to conductive, doped organic materials, in particular conductive doped polymers.
  • the device is appropriately (depending on the application) structured, provided with contacts and finally sealed, since the lifetime of the devices according to the invention is shortened in the presence of water and/or air.
  • the organic electroluminescent device according to the invention is characterised in that one or more layers are coated by means of a sublimation process, in which the materials are applied by vapour deposition in vacuum sublimation units at an initial pressure of less than 10 -5 mbar, preferably less than 10 -6 mbar.
  • the initial pressure it is also possible here for the initial pressure to be even lower, for example less than 10 -7 mbar.
  • an organic electroluminescent device characterised in that one or more layers are coated by means of the OVPD (organic vapour phase deposition) process or with the aid of carrier-gas sublimation, in which the materials are applied at a pressure of between 10 -5 mbar and 1 bar.
  • OVPD organic vapour phase deposition
  • carrier-gas sublimation in which the materials are applied at a pressure of between 10 -5 mbar and 1 bar.
  • OVJP organic vapour jet printing
  • an organic electroluminescent device characterised in that one or more layers are produced from solution, such as, for example, by spin coating, or by means of any desired printing process, such as, for example, screen printing, flexographic printing, nozzle printing or offset printing, but particularly preferably LITI (light induced thermal imaging, thermal transfer printing) or ink-jet printing.
  • Soluble compounds of the formula (I) are necessary for this purpose. High solubility can be achieved through suitable substitution of the compounds.
  • hybrid processes in which, for example, one or more layers are applied from solution and one or more further layers are applied by vapour deposition.
  • These processes are generally known to the person skilled in the art and can be applied by him without inventive step to organic electroluminescent devices comprising the compounds according to the invention.
  • the electronic devices comprising one or more compounds according to the invention can be employed in displays, as light sources in lighting applications and as light sources in medical and/or cosmetic applications (for example light therapy).
  • MeMgCI (461 mL, 3 M in THF, 1.38 mol) is added dropwise to a pre-cooled THF suspension (0 °C, 1.5 L) of compound I-a (135 g, 0.4 mol) and CeCl 3 (199 g, 0.8 mol).
  • a saturated aqueous solution of NH 4 Cl is added to quench the excess of MeMgCl, and the organic phase is extracted three times with ethyl acetate. The organic fractions are combined and washed with water and brine, successively. The volatiles were removed in vacuum to yield the desired product. 129 g (96 %).
  • Intermediate VI-a can be prepared in a similar manner as intermediate II-a starting from V-a (28.0 g, 61.8 mmol), MeMgCI (71 mL, 3 M in THF, 213 mmol) and CeCl 3 (30,5 g, 124 mmol) in 350 mL of THF. Yield: 25.5 g (91 %).
  • Intermediate VII-a can be synthesized following the same procedure as intermediate III-a starting from 25 g (55 mmol) of VI-a and 12 g of Amberlyst-15 in 300 mL of toluene. Yield: 20.4 g (85%).
  • IX-a and IX-b can be synthesized in analogous manner like BB-V by using CAS 1010100-76-1 as boronate ester starting material.
  • BB-XI.a and BB-XI.b can be synthesized in analogous manner like BB-V by using CAS 1010100-76-1 as boronate ester starting material.
  • inventive material combinations are used in the following layer sequence:
  • Glass plates coated with structured ITO (indium tin oxide) in a thickness of 50 nm serve as substrate. These are coated with the buffer (PEDOT) Clevios P VP AI 4083 (Heraeus Clevios GmbH, Leverkusen). The spin coating of the buffer is carried out from water in air. The layer is subsequently dried by heating at 180°C for 10 minutes. The hole transport layers and the emission layers are applied to the glass plates coated in this way.
  • PEDOT buffer
  • P VP AI 4083 Heraeus Clevios GmbH, Leverkusen
  • the hole-transport layer is the polymer of the structure shown in table 1, which was synthesised in accordance with WO2013156130 .
  • the polymer is dissolved in toluene, so that the solution typically has a solid content of approx. 5 g/l if, as here, the layer thickness of 20 nm which is typical for a device is to be achieved by means of spin coating.
  • the layers are applied by spin coating in an inert-gas atmosphere and dried by heating at 220°C for 30 min.
  • the emission layer is composed of the matrix material (host material) H and the emitting dopant (emitter) D. Both materials are present in the emission layer in a proportion of 92 % by weight H and 8 % by weight D.
  • the mixture for the emission layer is dissolved in toluene.
  • the solids content of such solutions is about 14 mg/ml if, as here, the layer thickness of 40 nm which is typical for a device is to be achieved by means of spin coating.
  • the layers are applied by spin coating in an inert-gas atmosphere, and dried by heating at 170°C for 10 minutes.
  • Table 1 Structural formulae of the materials used for the solution processed OLED layers HTL H SdT D1 D2 D3
  • the materials for the electron-blocking layer and the electron-transporting layer are likewise applied by thermal vapour deposition in a vacuum chamber and are shown in table 2.
  • the electron-blocking layer consists of the material ETM1 and the electron-transporting layer consists of the two materials ETM1 and ETM2, which are mixed with one another in a proportion by volume of 50% each by co-evaporation.
  • the cathode is formed by the thermal evaporation of an aluminium layer with a thickness of 100 nm.
  • the OLEDs are characterised by standard methods.
  • the electroluminescence spectra are recorded, the current efficiency (measured in cd/A) and the external quantum efficiency (EQE, measured in percent) as a function of the luminous density assuming Lambert emission characteristics are calculated from current/voltage/luminous density characteristic lines (IUL characteristic lines).
  • the electroluminescence spectra are recorded at a luminous density of 500 cd/m 2 , and the CIE 1931 x and y colour coordinates are calculated from this data.
  • the lifetime LT80 @ 500 cd/m 2 is defined as the time after which the initial luminous density of 500 cd/m 2 has dropped by 20%.
  • Table 2 Chemical structures of the materials used for thermally evaporated OLED layers ETM1 ETM2
  • inventive compounds are especially suitable as a dopant (emitter) when blended into a fluorescent blue matrix to form the emissive layer of a fluorescent blue OLED device.
  • the representative examples are D1, D2 and D3.
  • the properties of the various OLEDs are summarised in table 3.
  • Example V1 represents the prior art, whereas examples E2, E3 and E4 show properties of OLEDs containing materials of the present invention.
  • Table 3 Device data of solution processed OLEDs Example Host Dopant EQE @ 500 cd/m 2 LT80 @ 500 cd/m 2 CIE 92% 8% % h x y V1 H SdT 3.7 800 0.14 0.18 E2 H D1 3.6 1000 0.15 0.16 E3 H D2 3.8 1150 0.14 0.17 E4 H D3 5.2 1450 0.13 0.19
  • Table 3 shows that use of materials D1, D2 and D3 according to the present invention gives rise to improvements over the prior art (SdT) when used as fluorescent blue emitters, in particular with respect to lifetime.

Landscapes

  • Chemical & Material Sciences (AREA)
  • Organic Chemistry (AREA)
  • Engineering & Computer Science (AREA)
  • Materials Engineering (AREA)
  • Physics & Mathematics (AREA)
  • Spectroscopy & Molecular Physics (AREA)
  • Electroluminescent Light Sources (AREA)
  • Plural Heterocyclic Compounds (AREA)
  • Heterocyclic Carbon Compounds Containing A Hetero Ring Having Oxygen Or Sulfur (AREA)
  • Semiconductor Lasers (AREA)

Claims (16)

  1. Verbindung der Formel (1),
    Figure imgb0211
     wobei für die verwendeten Symbole und Indizes Folgendes gilt:
    ArN ist ein aromatisches oder heteroaromatisches Ringsystem mit 5 bis 60 aromatischen Ringatomen, das jeweils durch einen oder mehrere Reste R substituiert sein kann;
    E1 ist bei jedem Auftreten gleich oder verschieden aus - BR0-, -C(R0)2-, -C(R0)2-C(R0)2-, -C(R0)2-O-, -C(R0)2-S-, -R0C=CR0-, -R0C=N-, Si (R0) 2, -Si (R0) 2-Si (R0) 2-, -C(=O)-, -C(=NR0) -, -C(=C(R0)2)-, -O-, -S-, -S(=O)-, -SO2-, -N(R0)-, -P(R0)- und -P((=O)R0)- ausgewählt; oder E1 ist eine Gruppe der Formel (E-1),
    Figure imgb0212
     wobei das Symbol * in Formel (E-1) die entsprechende Gruppe E1 in Formel (1) anzeigt; und
    E0 ist bei jedem Auftreten gleich oder verschieden aus der Gruppe bestehend aus einer Einfachbindung, -BR0-, -C(R0)2-, -C(R0)2-C(R0)2-, -C(R0)2-O-, -C(R0)2-S-, -R0C=CR0-, -R0C=N-, Si(R0)2, -Si(R0)2-Si(R0)2-, -C(=O)-, -C(=NR0) -, -C(=C(R0)2)-, -O-, -S-, -S(=O)-, -SO2-, -N(R0)-, -P(R0)- und -P((=O)R0)- ausgewählt;
    E2 ist bei jedem Auftreten gleich oder verschieden aus der Gruppe bestehend aus -O-, -S-, -S(=O)- und -SO2-ausgewählt;
    R0 bis R5 stehen bei jedem Auftreten gleich oder verschieden für H, D, F, Cl, Br, I, CHO, CN, N(Ar)2, C(=0)Ar, P(=O) (Ar) 2, S(=O)Ar, S(=O)2Ar, NO2, Si(R)3, B(OR)2, OSO2R, eine geradkettige Alkyl-, Alkoxy- oder Thioalkylgruppe mit 1 bis 40 C-Atomen oder verzweigte oder cyclische Alkyl-, Alkoxy- oder Thioalkylgruppe mit 3 bis 40 C-Atomen, wobei jede dieser Gruppen durch einen oder mehrere Reste R substituiert sein kann, wobei jeweils eine oder mehrere nicht benachbarte CH2-Gruppen durch RC=CR, C=C, Si(R)2, Ge(R)2, Sn(R)2, C=O, C=S, C=Se, P(=O)(R), SO, SO2, O, S oder CONR ersetzt sein können und wobei ein oder mehrere H-Atome durch D, F, Cl, Br, I, CN oder NO2 ersetzt sein können, ein aromatisches oder heteroaromatisches Ringsystem mit 5 bis 60 aromatischen Ringatomen, das jeweils durch einen oder mehrere Reste R substituiert sein kann, oder eine Aryloxygruppe mit 5 bis 60 aromatischen Ringatomen, die durch einen oder mehrere Reste R substituiert sein kann, wobei zwei benachbarte Substituenten R0 und/oder zwei benachbarte Substituenten R1 und/oder zwei benachbarte Substituenten R2 und/oder zwei benachbarte Substituenten R3 und/oder zwei benachbarte Substituenten R4 und/oder zwei benachbarte Substituenten R5 ein mono- oder polycyclisches, aliphatisches Ringsystem oder aromatisches Ringsystem, das durch einen oder mehrere Reste R substituiert sein kann, bilden können;
    m, n, q stehen bei jedem Auftreten gleich oder verschieden für eine ganze Zahl, die aus 0, 1, 2, 3 oder 4 ausgewählt ist;
    p steht bei jedem Auftreten gleich oder verschieden für eine ganze Zahl, die aus 0, 1, 2 oder 3 ausgewählt ist; r steht bei jedem Auftreten gleich oder verschieden für eine ganze Zahl, die aus 0, 1 oder 2 ausgewählt ist;
    R steht bei jedem Auftreten gleich oder verschieden für H, D, F, Cl, Br, I, CHO, CN, N(Ar)2, C(=O)Ar, P(=O)(Ar)2, S(=O)Ar, S(=O)2Ar, NO2, Si(R')3, B(OR')2, OSO2R', eine geradkettige Alkyl-, Alkoxy- oder Thioalkylgruppe mit 1 bis 40 C-Atomen oder verzweigte oder cyclische Alkyl-, Alkoxy- oder Thioalkylgruppe mit 3 bis 40 C-Atomen, wobei jede dieser Gruppen durch einen oder mehrere Reste R substituiert sein kann, wobei jeweils eine oder mehrere nicht benachbarte CH2-Gruppen durch R'C=CR', C=C, Si(R')2, Ge(R')2, Sn(R')2, C=O, C=S, C=Se, P(=O) (R'), SO, SO2, O, S oder CONR' ersetzt sein können und wobei ein oder mehrere H-Atome durch D, F, Cl, Br, I, CN oder NO2 ersetzt sein können, ein aromatisches oder heteroaromatisches Ringsystem mit 5 bis 60 aromatischen Ringatomen, das jeweils durch einen oder mehrere Reste R' substituiert sein kann, oder eine Aryloxygruppe mit 5 bis 60 aromatischen Ringatomen, die durch einen oder mehrere Reste R' substituiert sein kann, wobei zwei benachbarte Substituenten R ein mono- oder polycyclisches, aliphatisches Ringsystem oder aromatisches Ringsystem, das durch einen oder mehrere Reste R' substituiert sein kann, bilden können;
    Ar ist ein aromatisches oder heteroaromatisches Ringsystem mit 5 bis 24 aromatischen Ringatomen, das jeweils auch durch einen oder mehrere Reste R' substituiert sein kann;
    R' steht bei jedem Auftreten gleich oder verschieden für H, D, F, Cl, Br, I, CN, eine geradkettige Alkyl-, Alkoxy- oder Thioalkylgruppe mit 1 bis 20 C-Atomen oder verzweigte oder cyclische Alkyl-, Alkoxy- oder Thioalkylgruppe mit 3 bis 20 C-Atomen, wobei jeweils eine oder mehrere nicht benachbarte CH2-Gruppen durch SO, SO2, O, S ersetzt sein können und wobei ein oder mehrere H-Atome durch D, F, Cl, Br oder I ersetzt sein können, oder ein aromatisches oder heteroaromatisches Ringsystem mit 5 bis 24 C-Atomen.
  2. Verbindung nach Anspruch 1, dadurch gekennzeichnet, dass ArN für Phenyl, Biphenyl, Fluoren, Spirobifluoren, Naphthalin, Phenanthren, Dibenzofuran, Dibenzothiophen, Carbazol, Pyridin, Pyrimidin, Pyrazin, Pyridazin, Triazin, Benzopyridin, Benzopyridazin, Benzopyrimidin oder Chinazolin oder für eine Kombination von zwei bis sechs dieser Gruppen, die jeweils durch einen oder mehrere Reste R substituiert sein können, steht.
  3. Verbindung nach Anspruch 1 oder 2, dadurch gekennzeichnet, dass ArN für Phenyl, Biphenyl, Fluoren, naphthalin, Phenanthren, Dibenzofuran, Dibenzothiophen, Carbazol oder für eine Kombination von zwei bis sechs dieser Gruppen, die jeweils durch einen oder mehrere Reste R substituiert sein können, steht.
  4. Verbindung nach einem oder mehreren der vorhergehenden Ansprüche, dadurch gekennzeichnet, dass sie aus Verbindungen der Formel (2) ausgewählt ist,
    Figure imgb0213
     wobei die Symbole ArN, E1, E2, R1 bis R5 und die Indizes m, n, p, q und r die gleiche Bedeutung wie in Anspruch 1 haben.
  5. Verbindung nach einem oder mehreren der vorhergehenden Ansprüche, die aus Verbindungen der Formel (3) ausgewählt ist,
    Figure imgb0214
     wobei die Symbole ArN, E2, R0, R1 bis R5 und die Indizes m, n, p, q und r die gleiche Bedeutung wie in Anspruch 1 haben.
  6. Verbindung nach einem oder mehreren der vorhergehenden Ansprüche, die aus Verbindungen der Formel (4) ausgewählt ist,
    Figure imgb0215
     wobei die Symbole ArN, E2, R0, R1 bis R5 und die Indizes m, n, p, q und r die gleiche Bedeutung wie in Anspruch 1 haben.
  7. Verbindung nach einem oder mehreren der vorhergehenden Ansprüche, dadurch gekennzeichnet, dass sie aus den Verbindungen der Formel (4-1) bis (4-4) ausgewählt ist,
    Figure imgb0216
    Figure imgb0217
    Figure imgb0218
    Figure imgb0219
     wobei die Symbole ArN, E2, R0, R1 bis R5 die gleiche Bedeutung wie in Anspruch 1 haben.
  8. Verbindung nach einem oder mehreren der vorhergehenden Ansprüche, dadurch gekennzeichnet, dass sie aus den Verbindungen der Formel (4-1a) bis (4-4a) ausgewählt ist,
    Figure imgb0220
    Figure imgb0221
    Figure imgb0222
    Figure imgb0223
     wobei die Symbole ArN, E2, R0 und R1 die gleiche Bedeutung wie in Anspruch 1 haben.
  9. Verbindung nach einem oder mehreren der vorhergehenden Ansprüche, dadurch gekennzeichnet, dass sie aus den Verbindungen der Formel (4-1b) bis (4-4b) ausgewählt ist,
    Figure imgb0224
    Figure imgb0225
    Figure imgb0226
    Figure imgb0227
     wobei die Symbole ArN, E2, R1 und R0 die gleiche Bedeutung wie in Anspruch 1 haben.
  10. Verbindung nach einem oder mehreren der vorhergehenden Ansprüche, dadurch gekennzeichnet, dass sie aus den Verbindungen der Formel (4-1c) bis (4-4c) ausgewählt ist,
    Figure imgb0228
    Figure imgb0229
    Figure imgb0230
    Figure imgb0231
     wobei die Symbole ArN, E2, R1 und R0 die gleiche Bedeutung wie in Anspruch 1 haben.
  11. Verbindung nach einem oder mehreren der vorhergehenden Ansprüche, dadurch gekennzeichnet, dass sie mindestens eine Gruppe R1 umfasst, die aus einem aromatischen oder heteroaromatischen Ringsystem mit 5 bis 60 aromatischen Ringatomen ausgewählt ist.
  12. Verbindung nach einem oder mehreren der vorhergehenden Ansprüche, dadurch gekennzeichnet, dass E2 für O steht.
  13. Polymer, Oligomer oder Dendrimer, enthaltend eine oder mehrere Verbindungen nach Anspruch 1, wobei die Bindung bzw. die Bindungen zum Polymer, Oligomer oder Dendrimer in beliebigen Positionen in Formel (1), die durch R0, R1, R2, R3, R4 oder R5 substituiert ist, lokalisiert sein kann bzw. können.
  14. Formulierung, umfassend mindestens eine Verbindung nach einem oder mehreren der Ansprüche 1 bis 12 oder mindestens ein Polymer, Oligomer oder Dendrimer nach Anspruch 13 und mindestens ein Lösungsmittel.
  15. Elektronische Vorrichtung, umfassend mindestens eine Verbindung nach einem oder mehreren der Ansprüche 1 bis 12 oder mindestens ein Polymer, Oligomer oder Dendrimer nach Anspruch 13, ausgewählt aus der Gruppe bestehend aus organischen Elektrolumineszenzvorrichtungen, organischen integrierten Schaltungen, organischen Feldeffekttransistoren, organischen Dünnfilmtransistoren, organischen lichtemittierenden Transistoren, organischen Solarzellen, farbstoffsensibilisierten organischen Solarzellen, organischen optischen Detektoren, organischen Photorezeptoren, organischen Feld-Quench-Devices, lichtemittierenden elektrochemischen Zellen, organischen Laserdioden und "Organic Plasmon Emitting Devices".
  16. Elektronische Vorrichtung nach Anspruch 15, bei der es sich um eine organische Elektrolumineszenzvorrichtung handelt, dadurch gekennzeichnet, dass die Verbindung nach einem oder mehreren der Ansprüche 1 bis 12 oder das Polymer, Oligomer oder Dendrimer nach Anspruch 13 als fluoreszierender Emitter oder als Matrixmaterial für fluoreszierende Emitter eingesetzt wird.
EP19756194.7A 2018-08-28 2019-08-26 Materialien für organische elektrolumineszente vorrichtungen Active EP3844242B1 (de)

Applications Claiming Priority (2)

Application Number Priority Date Filing Date Title
EP18191164 2018-08-28
PCT/EP2019/072662 WO2020043640A1 (en) 2018-08-28 2019-08-26 Materials for organic electroluminescent devices

Publications (2)

Publication Number Publication Date
EP3844242A1 EP3844242A1 (de) 2021-07-07
EP3844242B1 true EP3844242B1 (de) 2022-06-22

Family

ID=63442466

Family Applications (1)

Application Number Title Priority Date Filing Date
EP19756194.7A Active EP3844242B1 (de) 2018-08-28 2019-08-26 Materialien für organische elektrolumineszente vorrichtungen

Country Status (6)

Country Link
US (1) US20220140248A1 (de)
EP (1) EP3844242B1 (de)
KR (1) KR20210052488A (de)
CN (1) CN112567005B (de)
TW (1) TWI823993B (de)
WO (1) WO2020043640A1 (de)

Families Citing this family (7)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
EP4079742A1 (de) 2021-04-14 2022-10-26 Merck Patent GmbH Metallkomplexe
WO2023036976A1 (en) 2021-09-13 2023-03-16 Merck Patent Gmbh Materials for organic electroluminescent devices
WO2023208899A1 (en) 2022-04-28 2023-11-02 Merck Patent Gmbh Materials for organic electroluminescent devices
WO2024002629A1 (de) * 2022-06-28 2024-01-04 Merck Patent Gmbh Verbindungen für elektronische vorrichtungen
WO2024033282A1 (en) 2022-08-09 2024-02-15 Merck Patent Gmbh Materials for organic electroluminescent devices
WO2024115426A1 (de) * 2022-12-01 2024-06-06 Merck Patent Gmbh Polymere enthaltend spirotruxenderivate als wiederholungseinheit sowie elektrolumineszenzvorrichtungen enthaltend diese polymere
WO2024132892A1 (en) 2022-12-19 2024-06-27 Merck Patent Gmbh Materials for organic electroluminescent devices

Family Cites Families (105)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US4539507A (en) 1983-03-25 1985-09-03 Eastman Kodak Company Organic electroluminescent devices having improved power conversion efficiencies
US5061569A (en) 1990-07-26 1991-10-29 Eastman Kodak Company Electroluminescent device with organic electroluminescent medium
JP3295088B2 (ja) 1993-09-29 2002-06-24 出光興産株式会社 有機エレクトロルミネッセンス素子
JPH07133483A (ja) 1993-11-09 1995-05-23 Shinko Electric Ind Co Ltd Ｅｌ素子用有機発光材料及びｅｌ素子
DE59510315D1 (de) 1994-04-07 2002-09-19 Covion Organic Semiconductors Spiroverbindungen und ihre Verwendung als Elektrolumineszenzmaterialien
JP3302945B2 (ja) 1998-06-23 2002-07-15 ネースディスプレイ・カンパニー・リミテッド 新規な有機金属発光物質およびそれを含む有機電気発光素子
WO2000070655A2 (en) 1999-05-13 2000-11-23 The Trustees Of Princeton University Very high efficiency organic light emitting devices based on electrophosphorescence
EP2270895A3 (de) 1999-12-01 2011-03-30 The Trustees of Princeton University Komplexe für OLED-Anwendungen
KR100377321B1 (ko) 1999-12-31 2003-03-26 주식회사 엘지화학 피-형 반도체 성질을 갖는 유기 화합물을 포함하는 전기소자
US6660410B2 (en) 2000-03-27 2003-12-09 Idemitsu Kosan Co., Ltd. Organic electroluminescence element
US20020121638A1 (en) 2000-06-30 2002-09-05 Vladimir Grushin Electroluminescent iridium compounds with fluorinated phenylpyridines, phenylpyrimidines, and phenylquinolines and devices made with such compounds
KR100884039B1 (ko) 2000-08-11 2009-02-19 더 트러스티즈 오브 프린스턴 유니버시티 유기 금속 화합물 및 방사-이동 유기 전기인광
JP4154139B2 (ja) 2000-09-26 2008-09-24 キヤノン株式会社 発光素子
JP4154138B2 (ja) 2000-09-26 2008-09-24 キヤノン株式会社 発光素子、表示装置及び金属配位化合物
JP4154140B2 (ja) 2000-09-26 2008-09-24 キヤノン株式会社 金属配位化合物
KR100691543B1 (ko) 2002-01-18 2007-03-09 주식회사 엘지화학 새로운 전자 수송용 물질 및 이를 이용한 유기 발광 소자
ITRM20020411A1 (it) 2002-08-01 2004-02-02 Univ Roma La Sapienza Derivati dello spirobifluorene, loro preparazione e loro uso.
EP1549112A4 (de) 2002-09-20 2009-01-07 Idemitsu Kosan Co Organisches elektrolumineszenzelement
DE10249723A1 (de) 2002-10-25 2004-05-06 Covion Organic Semiconductors Gmbh Arylamin-Einheiten enthaltende konjugierte Polymere, deren Darstellung und Verwendung
US20060063027A1 (en) 2002-12-23 2006-03-23 Covion Organic Semiconductors Gmbh Organic electroluminescent element
DE10310887A1 (de) 2003-03-11 2004-09-30 Covion Organic Semiconductors Gmbh Matallkomplexe
US7851071B2 (en) 2003-03-13 2010-12-14 Idemitsu Kosan Co., Ltd. Nitrogen-containing heterocycle derivative and organic electroluminescent element using the same
JP4411851B2 (ja) 2003-03-19 2010-02-10 コニカミノルタホールディングス株式会社 有機エレクトロルミネッセンス素子
EP1717291A3 (de) 2003-04-15 2007-03-21 Merck Patent GmbH Mischungen von organischen, zur Emission befähigten Halbleitern und Maxtrixmaterialien, deren Verwendung und diese Mischungen enthaltende Elektronikbauteile
WO2004095889A1 (ja) 2003-04-23 2004-11-04 Konica Minolta Holdings, Inc. 有機エレクトロルミネッセンス素子及び表示装置
DE10333232A1 (de) 2003-07-21 2007-10-11 Merck Patent Gmbh Organisches Elektrolumineszenzelement
DE10338550A1 (de) 2003-08-19 2005-03-31 Basf Ag Übergangsmetallkomplexe mit Carbenliganden als Emitter für organische Licht-emittierende Dioden (OLEDs)
DE10345572A1 (de) 2003-09-29 2005-05-19 Covion Organic Semiconductors Gmbh Metallkomplexe
US7795801B2 (en) 2003-09-30 2010-09-14 Konica Minolta Holdings, Inc. Organic electroluminescent element, illuminator, display and compound
DE102004008304A1 (de) 2004-02-20 2005-09-08 Covion Organic Semiconductors Gmbh Organische elektronische Vorrichtungen
KR20060135801A (ko) 2004-03-05 2006-12-29 이데미쓰 고산 가부시키가이샤 유기 전계 발광 소자 및 유기 전계 발광 표시 장치
US7790890B2 (en) 2004-03-31 2010-09-07 Konica Minolta Holdings, Inc. Organic electroluminescence element material, organic electroluminescence element, display device and illumination device
KR100787425B1 (ko) 2004-11-29 2007-12-26 삼성에스디아이 주식회사 페닐카바졸계 화합물 및 이를 이용한 유기 전계 발광 소자
DE102004023277A1 (de) 2004-05-11 2005-12-01 Covion Organic Semiconductors Gmbh Neue Materialmischungen für die Elektrolumineszenz
US7598388B2 (en) 2004-05-18 2009-10-06 The University Of Southern California Carbene containing metal complexes as OLEDs
JP4862248B2 (ja) 2004-06-04 2012-01-25 コニカミノルタホールディングス株式会社 有機エレクトロルミネッセンス素子、照明装置及び表示装置
ITRM20040352A1 (it) 2004-07-15 2004-10-15 Univ Roma La Sapienza Derivati oligomerici dello spirobifluorene, loro preparazione e loro uso.
EP1655359A1 (de) 2004-11-06 2006-05-10 Covion Organic Semiconductors GmbH Organische Elektrolumineszenzvorrichtung
KR20090040398A (ko) 2005-03-18 2009-04-23 이데미쓰 고산 가부시키가이샤 방향족 아민 유도체 및 그것을 사용한 유기 전기발광 소자
KR101346907B1 (ko) 2005-04-14 2014-01-02 메르크 파텐트 게엠베하 유기 전자 소자용 화합물
KR101289923B1 (ko) 2005-05-03 2013-07-25 메르크 파텐트 게엠베하 유기 전계발광 장치 및 그에 사용되는 붕산 및 보린산유도체
DE102005023437A1 (de) 2005-05-20 2006-11-30 Merck Patent Gmbh Verbindungen für organische elektronische Vorrichtungen
CN102633820B (zh) 2005-12-01 2015-01-21 新日铁住金化学株式会社 有机电致发光元件用化合物及有机电致发光元件
GB0526185D0 (en) * 2005-12-22 2006-02-01 Cambridge Display Tech Ltd Electronic device
WO2007077766A1 (ja) 2005-12-27 2007-07-12 Idemitsu Kosan Co., Ltd. 有機エレクトロルミネッセンス素子用材料及び有機エレクトロルミネッセンス素子
DE102006025777A1 (de) 2006-05-31 2007-12-06 Merck Patent Gmbh Neue Materialien für organische Elektrolumineszenzvorrichtungen
DE102006025846A1 (de) 2006-06-02 2007-12-06 Merck Patent Gmbh Neue Materialien für organische Elektrolumineszenzvorrichtungen
DE102006031990A1 (de) 2006-07-11 2008-01-17 Merck Patent Gmbh Neue Materialien für organische Elektrolumineszenzvorrichtungen
JP4388590B2 (ja) 2006-11-09 2009-12-24 新日鐵化学株式会社 有機電界発光素子用化合物及び有機電界発光素子
DE102007002714A1 (de) 2007-01-18 2008-07-31 Merck Patent Gmbh Neue Materialien für organische Elektrolumineszenzvorrichtungen
US8044390B2 (en) 2007-05-25 2011-10-25 Idemitsu Kosan Co., Ltd. Material for organic electroluminescent device, organic electroluminescent device, and organic electroluminescent display
DE102007024850A1 (de) 2007-05-29 2008-12-04 Merck Patent Gmbh Neue Materialien für organische Elektrolumineszenzvorrichtungen
DE102007031220B4 (de) 2007-07-04 2022-04-28 Novaled Gmbh Chinoide Verbindungen und deren Verwendung in halbleitenden Matrixmaterialien, elektronischen und optoelektronischen Bauelementen
EP2045848B1 (de) 2007-07-18 2017-09-27 Idemitsu Kosan Co., Ltd. Material für ein organisches elektrolumineszenzgerät und organisches elektrolumineszenzgerät
DE102007053771A1 (de) 2007-11-12 2009-05-14 Merck Patent Gmbh Organische Elektrolumineszenzvorrichtungen
US7862908B2 (en) 2007-11-26 2011-01-04 National Tsing Hua University Conjugated compounds containing hydroindoloacridine structural elements, and their use
EP2213662B1 (de) 2007-11-30 2012-04-18 Idemitsu Kosan Co., Ltd. Azaindenofluorendionderivat, material für ein organisches elektrolumineszierendes gerät und organisches lumineszierendes gerät
TWI478624B (zh) 2008-03-27 2015-03-21 Nippon Steel & Sumikin Chem Co Organic electroluminescent elements
US8057712B2 (en) 2008-04-29 2011-11-15 Novaled Ag Radialene compounds and their use
DE102008033943A1 (de) 2008-07-18 2010-01-21 Merck Patent Gmbh Neue Materialien für organische Elektrolumineszenzvorrichtungen
DE102008035413A1 (de) 2008-07-29 2010-02-04 Merck Patent Gmbh Verbindungen für organische elektronische Vorrichtungen
DE102008036982A1 (de) 2008-08-08 2010-02-11 Merck Patent Gmbh Organische Elektrolumineszenzvorrichtung
US8119037B2 (en) 2008-10-16 2012-02-21 Novaled Ag Square planar transition metal complexes and organic semiconductive materials using them as well as electronic or optoelectric components
KR101506919B1 (ko) 2008-10-31 2015-03-30 롬엔드하스전자재료코리아유한회사 신규한 유기 전자재료용 화합물 및 이를 포함하는 유기 전자 소자
KR20110097612A (ko) 2008-11-11 2011-08-31 메르크 파텐트 게엠베하 유기 전계발광 소자
DE102008056688A1 (de) 2008-11-11 2010-05-12 Merck Patent Gmbh Materialien für organische Elektrolumineszenzvorrichtungen
DE102008064200A1 (de) 2008-12-22 2010-07-01 Merck Patent Gmbh Organische Elektrolumineszenzvorrichtung
DE102009009277B4 (de) 2009-02-17 2023-12-07 Merck Patent Gmbh Organische elektronische Vorrichtung, Verfahren zu deren Herstellung und Verwendung von Verbindungen
US9156939B2 (en) 2009-02-27 2015-10-13 Merck Patent Gmbh Polymer containing aldehyde groups, reaction and crosslinking of this polymer, crosslinked polymer, and electroluminescent device comprising this polymer
DE102009014513A1 (de) 2009-03-23 2010-09-30 Merck Patent Gmbh Organische Elektrolumineszenzvorrichtung
DE102009023155A1 (de) 2009-05-29 2010-12-02 Merck Patent Gmbh Materialien für organische Elektrolumineszenzvorrichtungen
DE102009031021A1 (de) 2009-06-30 2011-01-05 Merck Patent Gmbh Materialien für organische Elektrolumineszenzvorrichtungen
DE102009048791A1 (de) 2009-10-08 2011-04-14 Merck Patent Gmbh Materialien für organische Elektrolumineszenzvorrichtungen
PL2513125T3 (pl) 2009-12-14 2015-04-30 Udc Ireland Ltd Kompleksy metali z ligandami diazabenzimidazolokarbenowymi i ich zastosowanie w OLED-ach
DE102010005697A1 (de) 2010-01-25 2011-07-28 Merck Patent GmbH, 64293 Verbindungen für elektronische Vorrichtungen
DE102010012738A1 (de) 2010-03-25 2011-09-29 Merck Patent Gmbh Materialien für organische Elektrolumineszenzvorrichtungen
DE102010013495A1 (de) 2010-03-31 2011-10-06 Siemens Aktiengesellschaft Dotierstoff für eine Lochleiterschicht für organische Halbleiterbauelemente und Verwendung dazu
DE102010019306B4 (de) 2010-05-04 2021-05-20 Merck Patent Gmbh Organische Elektrolumineszenzvorrichtungen
DE102010045405A1 (de) 2010-09-15 2012-03-15 Merck Patent Gmbh Materialien für organische Elektrolumineszenzvorrichtungen
DE102010048607A1 (de) 2010-10-15 2012-04-19 Merck Patent Gmbh Verbindungen für elektronische Vorrichtungen
DE102010048608A1 (de) 2010-10-15 2012-04-19 Merck Patent Gmbh Materialien für organische Elektrolumineszenzvorrichtungen
WO2012095143A1 (de) 2011-01-13 2012-07-19 Merck Patent Gmbh Verbindungen für organische elektrolumineszenzvorrichtungen
US9620722B2 (en) 2011-04-18 2017-04-11 Merck Patent Gmbh Materials for organic electroluminescent devices
JP6193215B2 (ja) 2011-05-05 2017-09-06 メルク パテント ゲーエムベーハー 電子デバイスのための化合物
RU2626977C2 (ru) 2011-09-21 2017-08-02 Мерк Патент Гмбх Производные карбазола для органических электролюминисцентных устройств
US10305040B2 (en) 2011-11-17 2019-05-28 Merck Patent Gmbh Spiro dihydroacridine derivatives and the use thereof as materials for organic electroluminescence devices
KR101605987B1 (ko) 2012-02-14 2016-03-23 메르크 파텐트 게엠베하 유기 전계발광 소자용 스피로비플루오렌 화합물
US9644070B2 (en) 2012-04-17 2017-05-09 Merck Patent Gmbh Cross-linkable and cross-linked polymers, process for the preparation thereof, and the use thereof
DE112013002910T5 (de) 2012-06-12 2015-03-19 Merck Patent Gmbh Verbindungen für elektronische Vorrichtungen
KR102284234B1 (ko) 2012-07-23 2021-07-30 메르크 파텐트 게엠베하 2-디아릴아미노플루오렌의 유도체 및 이를 함유하는 유기 전자 화합물
JP6219388B2 (ja) 2012-07-23 2017-10-25 メルク パテント ゲーエムベーハー フルオレンおよびそれらを含む有機電子素子
KR102337198B1 (ko) 2012-07-23 2021-12-09 메르크 파텐트 게엠베하 화합물 및 유기 전계 발광 디바이스
CN104684886B (zh) 2012-09-04 2017-07-18 默克专利有限公司 用于电子器件的化合物
CN104884572B (zh) 2013-01-03 2017-09-19 默克专利有限公司 用于电子器件的材料
JP6419802B2 (ja) 2013-10-14 2018-11-07 メルク、パテント、ゲゼルシャフト、ミット、ベシュレンクテル、ハフツングＭｅｒｃｋ Ｐａｔｅｎｔ ＧｍｂＨ 電子素子のための材料
CN106170476A (zh) 2014-04-16 2016-11-30 默克专利有限公司 用于电子器件的材料
US10487262B2 (en) 2015-03-25 2019-11-26 Merck Patent Gmbh Materials for organic electroluminescent devices
KR102002034B1 (ko) 2015-07-09 2019-07-22 에스에프씨주식회사 고효율과 장수명을 갖는 유기 발광 소자
CN107949561B (zh) 2015-08-14 2021-11-02 默克专利有限公司 用于有机电致发光器件的吩噁嗪衍生物
JP6843834B2 (ja) 2015-08-14 2021-03-17 メルク、パテント、ゲゼルシャフト、ミット、ベシュレンクテル、ハフツングＭｅｒｃｋ Ｐａｔｅｎｔ ＧｍｂＨ 有機エレクトロルミネッセンス素子のためのフェノキサジン誘導体
US20180327339A1 (en) 2015-08-28 2018-11-15 Merck Patent Gmbh Compounds for electronic devices
US11158816B2 (en) 2015-08-28 2021-10-26 Merck Patent Gmbh 6,9,15,18-tetrahydro-s-indaceno[1,2-b:5,6-b′]difluorene derivatives and use thereof in electronic devices
CN107573925B (zh) * 2016-07-05 2020-02-21 上海和辉光电有限公司 一种有机电致发光化合物
CN107573306B (zh) * 2016-07-05 2020-04-28 上海和辉光电有限公司 一种有机电致发光化合物
KR102259334B1 (ko) * 2016-11-23 2021-05-31 주식회사 엘지화학 전기활성 화합물

Also Published As

Publication number Publication date
CN112567005B (zh) 2024-04-16
CN112567005A (zh) 2021-03-26
EP3844242A1 (de) 2021-07-07
WO2020043640A1 (en) 2020-03-05
KR20210052488A (ko) 2021-05-10
TW202024045A (zh) 2020-07-01
US20220140248A1 (en) 2022-05-05
TWI823993B (zh) 2023-12-01

Similar Documents

Publication Publication Date Title
US11578063B2 (en) Materials for organic electroluminescent devices
EP3334731B1 (de) Phenoxazinderivate für organische elektrolumineszente vorrichtungen
EP3481796B1 (de) Materialien für organische elektrolumineszente vorrichtungen
KR102284234B1 (ko) 2-디아릴아미노플루오렌의 유도체 및 이를 함유하는 유기 전자 화합물
EP3844242B1 (de) Materialien für organische elektrolumineszente vorrichtungen
US20210005821A1 (en) Materials for organic electroluminescent devices
EP3844244B1 (de) Materialien für organische elektrolumineszente vorrichtungen
EP3844243B1 (de) Materialien für organische elektrolumineszente vorrichtungen
EP3250658B1 (de) Materialien für elektronische vorrichtungen
US11639339B2 (en) Materials for organic electroluminescent devices
US11939339B2 (en) Materials for organic electroluminescent devices
EP4126884A1 (de) Materialien für organische elektrolumineszenzvorrichtungen
WO2019170578A1 (en) Materials for organic electroluminescent devices
WO2022017997A1 (en) Materials for organic electroluminescent devices
EP4320648A1 (de) Materialien für organische elektrolumineszenzvorrichtungen

Legal Events

Date Code Title Description
STAA Information on the status of an ep patent application or granted ep patent

Free format text: STATUS: UNKNOWN

STAA Information on the status of an ep patent application or granted ep patent

Free format text: STATUS: THE INTERNATIONAL PUBLICATION HAS BEEN MADE

STAA Information on the status of an ep patent application or granted ep patent

Free format text: STATUS: REQUEST FOR EXAMINATION WAS MADE

PUAI Public reference made under article 153(3) epc to a published international application that has entered the european phase

Free format text: ORIGINAL CODE: 0009012

17P Request for examination filed

Effective date: 20210225

AK Designated contracting states

Kind code of ref document: A1

Designated state(s): AL AT BE BG CH CY CZ DE DK EE ES FI FR GB GR HR HU IE IS IT LI LT LU LV MC MK MT NL NO PL PT RO RS SE SI SK SM TR

DAV Request for validation of the european patent (deleted)
DAX Request for extension of the european patent (deleted)
GRAP Despatch of communication of intention to grant a patent

Free format text: ORIGINAL CODE: EPIDOSNIGR1

STAA Information on the status of an ep patent application or granted ep patent

Free format text: STATUS: GRANT OF PATENT IS INTENDED

RIC1 Information provided on ipc code assigned before grant

Ipc: C07D 307/77 20060101ALI20220113BHEP

Ipc: H01L 51/00 20060101ALI20220113BHEP

Ipc: C09K 11/06 20060101AFI20220113BHEP

INTG Intention to grant announced

Effective date: 20220131

GRAS Grant fee paid

Free format text: ORIGINAL CODE: EPIDOSNIGR3

GRAA (expected) grant

Free format text: ORIGINAL CODE: 0009210

STAA Information on the status of an ep patent application or granted ep patent

Free format text: STATUS: THE PATENT HAS BEEN GRANTED

AK Designated contracting states

Kind code of ref document: B1

Designated state(s): AL AT BE BG CH CY CZ DE DK EE ES FI FR GB GR HR HU IE IS IT LI LT LU LV MC MK MT NL NO PL PT RO RS SE SI SK SM TR

REG Reference to a national code

Ref country code: GB

Ref legal event code: FG4D

REG Reference to a national code

Ref country code: CH

Ref legal event code: EP

REG Reference to a national code

Ref country code: DE

Ref legal event code: R096

Ref document number: 602019016225

Country of ref document: DE

REG Reference to a national code

Ref country code: AT

Ref legal event code: REF

Ref document number: 1499778

Country of ref document: AT

Kind code of ref document: T

Effective date: 20220715

REG Reference to a national code

Ref country code: IE

Ref legal event code: FG4D

REG Reference to a national code

Ref country code: LT

Ref legal event code: MG9D

REG Reference to a national code

Ref country code: NL

Ref legal event code: MP

Effective date: 20220622

PG25 Lapsed in a contracting state [announced via postgrant information from national office to epo]

Ref country code: SE

Free format text: LAPSE BECAUSE OF FAILURE TO SUBMIT A TRANSLATION OF THE DESCRIPTION OR TO PAY THE FEE WITHIN THE PRESCRIBED TIME-LIMIT

Effective date: 20220622

Ref country code: NO

Free format text: LAPSE BECAUSE OF FAILURE TO SUBMIT A TRANSLATION OF THE DESCRIPTION OR TO PAY THE FEE WITHIN THE PRESCRIBED TIME-LIMIT

Effective date: 20220922

Ref country code: LT

Free format text: LAPSE BECAUSE OF FAILURE TO SUBMIT A TRANSLATION OF THE DESCRIPTION OR TO PAY THE FEE WITHIN THE PRESCRIBED TIME-LIMIT

Effective date: 20220622

Ref country code: HR

Free format text: LAPSE BECAUSE OF FAILURE TO SUBMIT A TRANSLATION OF THE DESCRIPTION OR TO PAY THE FEE WITHIN THE PRESCRIBED TIME-LIMIT

Effective date: 20220622

Ref country code: GR

Free format text: LAPSE BECAUSE OF FAILURE TO SUBMIT A TRANSLATION OF THE DESCRIPTION OR TO PAY THE FEE WITHIN THE PRESCRIBED TIME-LIMIT

Effective date: 20220923

Ref country code: FI

Free format text: LAPSE BECAUSE OF FAILURE TO SUBMIT A TRANSLATION OF THE DESCRIPTION OR TO PAY THE FEE WITHIN THE PRESCRIBED TIME-LIMIT

Effective date: 20220622

Ref country code: BG

Free format text: LAPSE BECAUSE OF FAILURE TO SUBMIT A TRANSLATION OF THE DESCRIPTION OR TO PAY THE FEE WITHIN THE PRESCRIBED TIME-LIMIT

Effective date: 20220922

REG Reference to a national code

Ref country code: AT

Ref legal event code: MK05

Ref document number: 1499778

Country of ref document: AT

Kind code of ref document: T

Effective date: 20220622

PG25 Lapsed in a contracting state [announced via postgrant information from national office to epo]

Ref country code: RS

Free format text: LAPSE BECAUSE OF FAILURE TO SUBMIT A TRANSLATION OF THE DESCRIPTION OR TO PAY THE FEE WITHIN THE PRESCRIBED TIME-LIMIT

Effective date: 20220622

Ref country code: LV

Free format text: LAPSE BECAUSE OF FAILURE TO SUBMIT A TRANSLATION OF THE DESCRIPTION OR TO PAY THE FEE WITHIN THE PRESCRIBED TIME-LIMIT

Effective date: 20220622

PG25 Lapsed in a contracting state [announced via postgrant information from national office to epo]

Ref country code: NL

Free format text: LAPSE BECAUSE OF FAILURE TO SUBMIT A TRANSLATION OF THE DESCRIPTION OR TO PAY THE FEE WITHIN THE PRESCRIBED TIME-LIMIT

Effective date: 20220622

PG25 Lapsed in a contracting state [announced via postgrant information from national office to epo]

Ref country code: SM

Free format text: LAPSE BECAUSE OF FAILURE TO SUBMIT A TRANSLATION OF THE DESCRIPTION OR TO PAY THE FEE WITHIN THE PRESCRIBED TIME-LIMIT

Effective date: 20220622

Ref country code: SK

Free format text: LAPSE BECAUSE OF FAILURE TO SUBMIT A TRANSLATION OF THE DESCRIPTION OR TO PAY THE FEE WITHIN THE PRESCRIBED TIME-LIMIT

Effective date: 20220622

Ref country code: RO

Free format text: LAPSE BECAUSE OF FAILURE TO SUBMIT A TRANSLATION OF THE DESCRIPTION OR TO PAY THE FEE WITHIN THE PRESCRIBED TIME-LIMIT

Effective date: 20220622

Ref country code: PT

Free format text: LAPSE BECAUSE OF FAILURE TO SUBMIT A TRANSLATION OF THE DESCRIPTION OR TO PAY THE FEE WITHIN THE PRESCRIBED TIME-LIMIT

Effective date: 20221024

Ref country code: ES

Free format text: LAPSE BECAUSE OF FAILURE TO SUBMIT A TRANSLATION OF THE DESCRIPTION OR TO PAY THE FEE WITHIN THE PRESCRIBED TIME-LIMIT

Effective date: 20220622

Ref country code: EE

Free format text: LAPSE BECAUSE OF FAILURE TO SUBMIT A TRANSLATION OF THE DESCRIPTION OR TO PAY THE FEE WITHIN THE PRESCRIBED TIME-LIMIT

Effective date: 20220622

Ref country code: CZ

Free format text: LAPSE BECAUSE OF FAILURE TO SUBMIT A TRANSLATION OF THE DESCRIPTION OR TO PAY THE FEE WITHIN THE PRESCRIBED TIME-LIMIT

Effective date: 20220622

Ref country code: AT

Free format text: LAPSE BECAUSE OF FAILURE TO SUBMIT A TRANSLATION OF THE DESCRIPTION OR TO PAY THE FEE WITHIN THE PRESCRIBED TIME-LIMIT

Effective date: 20220622

PG25 Lapsed in a contracting state [announced via postgrant information from national office to epo]

Ref country code: PL

Free format text: LAPSE BECAUSE OF FAILURE TO SUBMIT A TRANSLATION OF THE DESCRIPTION OR TO PAY THE FEE WITHIN THE PRESCRIBED TIME-LIMIT

Effective date: 20220622

Ref country code: IS

Free format text: LAPSE BECAUSE OF FAILURE TO SUBMIT A TRANSLATION OF THE DESCRIPTION OR TO PAY THE FEE WITHIN THE PRESCRIBED TIME-LIMIT

Effective date: 20221022

REG Reference to a national code

Ref country code: DE

Ref legal event code: R097

Ref document number: 602019016225

Country of ref document: DE

PG25 Lapsed in a contracting state [announced via postgrant information from national office to epo]

Ref country code: MC

Free format text: LAPSE BECAUSE OF FAILURE TO SUBMIT A TRANSLATION OF THE DESCRIPTION OR TO PAY THE FEE WITHIN THE PRESCRIBED TIME-LIMIT

Effective date: 20220622

Ref country code: AL

Free format text: LAPSE BECAUSE OF FAILURE TO SUBMIT A TRANSLATION OF THE DESCRIPTION OR TO PAY THE FEE WITHIN THE PRESCRIBED TIME-LIMIT

Effective date: 20220622

REG Reference to a national code

Ref country code: CH

Ref legal event code: PL

PG25 Lapsed in a contracting state [announced via postgrant information from national office to epo]

Ref country code: LU

Free format text: LAPSE BECAUSE OF NON-PAYMENT OF DUE FEES

Effective date: 20220826

Ref country code: LI

Free format text: LAPSE BECAUSE OF NON-PAYMENT OF DUE FEES

Effective date: 20220831

Ref country code: DK

Free format text: LAPSE BECAUSE OF FAILURE TO SUBMIT A TRANSLATION OF THE DESCRIPTION OR TO PAY THE FEE WITHIN THE PRESCRIBED TIME-LIMIT

Effective date: 20220622

Ref country code: CH

Free format text: LAPSE BECAUSE OF NON-PAYMENT OF DUE FEES

Effective date: 20220831

PLBE No opposition filed within time limit

Free format text: ORIGINAL CODE: 0009261

STAA Information on the status of an ep patent application or granted ep patent

Free format text: STATUS: NO OPPOSITION FILED WITHIN TIME LIMIT

REG Reference to a national code

Ref country code: BE

Ref legal event code: MM

Effective date: 20220831

26N No opposition filed

Effective date: 20230323

P01 Opt-out of the competence of the unified patent court (upc) registered

Effective date: 20230519

PG25 Lapsed in a contracting state [announced via postgrant information from national office to epo]

Ref country code: IE

Free format text: LAPSE BECAUSE OF NON-PAYMENT OF DUE FEES

Effective date: 20220826

Ref country code: FR

Free format text: LAPSE BECAUSE OF NON-PAYMENT OF DUE FEES

Effective date: 20220831

PG25 Lapsed in a contracting state [announced via postgrant information from national office to epo]

Ref country code: SI

Free format text: LAPSE BECAUSE OF FAILURE TO SUBMIT A TRANSLATION OF THE DESCRIPTION OR TO PAY THE FEE WITHIN THE PRESCRIBED TIME-LIMIT

Effective date: 20220622

PG25 Lapsed in a contracting state [announced via postgrant information from national office to epo]

Ref country code: BE

Free format text: LAPSE BECAUSE OF NON-PAYMENT OF DUE FEES

Effective date: 20220831

PGFP Annual fee paid to national office [announced via postgrant information from national office to epo]

Ref country code: DE

Payment date: 20230703

Year of fee payment: 5

PG25 Lapsed in a contracting state [announced via postgrant information from national office to epo]

Ref country code: IT

Free format text: LAPSE BECAUSE OF FAILURE TO SUBMIT A TRANSLATION OF THE DESCRIPTION OR TO PAY THE FEE WITHIN THE PRESCRIBED TIME-LIMIT

Effective date: 20220622

GBPC Gb: european patent ceased through non-payment of renewal fee

Effective date: 20230826

PG25 Lapsed in a contracting state [announced via postgrant information from national office to epo]

Ref country code: CY

Free format text: LAPSE BECAUSE OF FAILURE TO SUBMIT A TRANSLATION OF THE DESCRIPTION OR TO PAY THE FEE WITHIN THE PRESCRIBED TIME-LIMIT

Effective date: 20220622

PG25 Lapsed in a contracting state [announced via postgrant information from national office to epo]

Ref country code: MK

Free format text: LAPSE BECAUSE OF FAILURE TO SUBMIT A TRANSLATION OF THE DESCRIPTION OR TO PAY THE FEE WITHIN THE PRESCRIBED TIME-LIMIT

Effective date: 20220622

Ref country code: HU

Free format text: LAPSE BECAUSE OF FAILURE TO SUBMIT A TRANSLATION OF THE DESCRIPTION OR TO PAY THE FEE WITHIN THE PRESCRIBED TIME-LIMIT; INVALID AB INITIO

Effective date: 20190826

PG25 Lapsed in a contracting state [announced via postgrant information from national office to epo]

Ref country code: GB

Free format text: LAPSE BECAUSE OF NON-PAYMENT OF DUE FEES

Effective date: 20230826

PG25 Lapsed in a contracting state [announced via postgrant information from national office to epo]

Ref country code: GB

Free format text: LAPSE BECAUSE OF NON-PAYMENT OF DUE FEES

Effective date: 20230826

PG25 Lapsed in a contracting state [announced via postgrant information from national office to epo]

Ref country code: MT

Free format text: LAPSE BECAUSE OF FAILURE TO SUBMIT A TRANSLATION OF THE DESCRIPTION OR TO PAY THE FEE WITHIN THE PRESCRIBED TIME-LIMIT

Effective date: 20220622